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      Immunophysiology and Pathology of Inflammation in the Testis and Epididymis

      review-article
      1 ,
      Journal of Andrology
      Blackwell Publishing Ltd
      Sperm, autoimmunity, orchitis, epididymitis, leukocytes, antibodies

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          Abstract

          ABSTRACT: The ability of spermatogenic cells to evade the host immune system and the ability of systemic inflammation to inhibit male reproductive function represent two of the most intriguing conundrums of male reproduction. Clearly, an understanding of the underlying immunology of the male reproductive tract is crucial to resolving these superficially incompatible observations. One important consideration must be the very different immunological environments of the testis, where sperm develop, and the epididymis, where sperm mature and are stored. Compared with the elaborate blood‐testis barrier, the tight junctions of the epididymis are much less effective. Unlike the seminiferous epithelium, immune cells are commonly observed within the epithelium, and can even be found within the lumen, of the epididymis. Crucially, there is little evidence for extended allograft survival (immune privilege) in the epididymis, as it exists in the testis, and the epididymis is much more susceptible to loss of immune tolerance. Moreover, the incidence of epididymitis is considerably greater than that of orchitis in humans, and susceptibility to sperm antibody formation after damage to the epididymis or vas deferens increases with increasing distance of the damage from the testis. Although we still know relatively little about testicular immunity, we know less about the interactions between the epididymis and the immune system. Given that the epididymis appears to be more susceptible to inflammation and immune reactions than the testis, and thereby represents the weaker link in protecting developing sperm from the immune system, it is probably time this imbalance in knowledge was addressed.

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          Most cited references166

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          Aire regulates negative selection of organ-specific T cells.

          Autoimmune polyendocrinopathy syndrome type 1 is a recessive Mendelian disorder resulting from mutations in a novel gene, AIRE, and is characterized by a spectrum of organ-specific autoimmune diseases. It is not known what tolerance mechanisms are defective as a result of AIRE mutation. By tracing the fate of autoreactive CD4+ T cells with high affinity for a pancreatic antigen in transgenic mice with an Aire mutation, we show here that Aire deficiency causes almost complete failure to delete the organ-specific cells in the thymus. These results indicate that autoimmune polyendocrinopathy syndrome 1 is caused by failure of a specialized mechanism for deleting forbidden T cell clones, establishing a central role for this tolerance mechanism.
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            Mechanisms maintaining peripheral tolerance.

            The presentation of self-peptide-MHC complexes in the periphery to potentially autoreactive T cells that have escaped negative selection in the thymus poses an important problem to the immune system. In this review, I discuss data that reveal barriers preventing peripheral T cell recognition of self-peptide-MHC complexes, as well as the physiological mechanisms that ensure the elimination or functional inactivation (anergy) of T cells that do come to recognize self-peptide-MHC and threaten the health of the individual.
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              A role for CD95 ligand in preventing graft rejection.

              Testis is a remarkable immune-privileged site, long known for its ability to support allogeneic and xenogeneic tissue transplants. Here we have investigated the molecular basis for testis immune privilege. Testis grafts derived from mice that can express functional CD95 (Fas or Apo-1) ligand survived indefinitely when transplanted under the kidney capsule of allogeneic animals, whereas testis grafts derived from mutant gld mice, which express non-functional ligand, were rejected. Further analysis of testis showed that CD95 ligand messenger RNA is constitutively expressed by testicular Sertoli cells, and that Sertoli cells from normal mice, but not gld mice, were accepted when transplanted into allogeneic recipients. CD95 ligand expression in the testis probably acts by inducing apoptotic cell death of CD95-expressing, recipient T cells activated in response to graft antigens. These findings indicate that CD95 ligand could be used to create immune-privileged tissue for a variety of transplant uses.
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                Author and article information

                Journal
                J Androl
                J. Androl
                10.1002/(ISSN)1939-4640
                JAND
                Journal of Andrology
                Blackwell Publishing Ltd (Oxford, UK )
                0196-3635
                1939-4640
                02 January 2013
                Nov-Dec 2011
                : 32
                : 6 ( doiID: 10.1002/jand.2011.32.issue-6 )
                : 625-640
                Affiliations
                [ 1 ]Monash Institute of Medical Research, Monash University, Melbourne, Australia
                Author notes
                [*] [* ] Monash Institute of Medical Research, Monash University, 27‐31 Wright St, Clayton, Victoria 3168, Australia (e‐mail: mark.hedger@ 123456monash.edu ).
                Article
                JAND1486
                10.2164/jandrol.111.012989
                7166903
                21764900
                4d6db39b-47b3-4fb1-9f8d-7bbec22d6025
                2011 American Society of Andrology

                This article is being made freely available through PubMed Central as part of the COVID-19 public health emergency response. It can be used for unrestricted research re-use and analysis in any form or by any means with acknowledgement of the original source, for the duration of the public health emergency.

                History
                : 5 January 2011
                : 25 April 2011
                Page count
                links-crossref: 243, Figures: 1, Tables: 1, Equations: 0, References: 178, Pages: 16
                Categories
                Review
                Custom metadata
                2.0
                November‐December 2011
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.8.0 mode:remove_FC converted:15.04.2020

                sperm,autoimmunity,orchitis,epididymitis,leukocytes,antibodies
                sperm, autoimmunity, orchitis, epididymitis, leukocytes, antibodies

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